Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Beta-Alanine | HCID 239 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 57994057 | HCID 57994057 | — |
| Reactant | HCID 57994060 | HCID 57994060 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57994056 | HCID 57994056 | — |
Reaction Steps
To a mixture of 2-(5-oxo-2-thioxoimidazolidin-1-yl)-3-phenylpropanoic acid (0.044 g, 0.175 mmol) and 5-(4-bromo-3-chloro-phenyl)thiophene-2-carbaldehyde (0.050 g, 0.166 mmol) in acetic acid 5 mL is added β-alanine (1.6 mg, 0.01 r8 mmol) and heat to 170° C. for 30 min under microwave irradiation. The resulting reaction mixture is cooled down and the solvent is removed. The pure product (0.075 g, 0.141 mmol, red solid) is obtained by column chromatography using MeOH/DCM, 2-7% ration solvent system. 1H-NMR (CDCl3/300 MHz): 9.88 (br, 1H), 8.92 (br, 1H), 7.65 (m, 2H), 7.31 (m, 8H), 6.85 (s, 1H), 5.76 (dd, J=11.1, 5.4 Hz, 1H), 3.70 (m, 2H). MS (ES−, m/z): 545.2 (M−, 100.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759384B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-e5eab9dceb214be2964d79efb9c587ea |
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| Source note | uspto-grants-2014_06 |
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